[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

CN1776522A - Imaging compositions and methods - Google Patents

Imaging compositions and methods Download PDF

Info

Publication number
CN1776522A
CN1776522A CNA2005100656435A CN200510065643A CN1776522A CN 1776522 A CN1776522 A CN 1776522A CN A2005100656435 A CNA2005100656435 A CN A2005100656435A CN 200510065643 A CN200510065643 A CN 200510065643A CN 1776522 A CN1776522 A CN 1776522A
Authority
CN
China
Prior art keywords
image forming
forming composition
composition
perhaps
emulsion
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CNA2005100656435A
Other languages
Chinese (zh)
Other versions
CN1776522B (en
Inventor
R·K·巴尔
J·T·法西
C·奥科诺
J·G·谢尔诺特
J·J·皮斯科斯基
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Rohm and Haas Electronic Materials LLC
Original Assignee
Rohm and Haas Electronic Materials LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Rohm and Haas Electronic Materials LLC filed Critical Rohm and Haas Electronic Materials LLC
Publication of CN1776522A publication Critical patent/CN1776522A/en
Application granted granted Critical
Publication of CN1776522B publication Critical patent/CN1776522B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/72—Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705
    • G03C1/73—Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705 containing organic compounds
    • E—FIXED CONSTRUCTIONS
    • E05—LOCKS; KEYS; WINDOW OR DOOR FITTINGS; SAFES
    • E05D—HINGES OR SUSPENSION DEVICES FOR DOORS, WINDOWS OR WINGS
    • E05D15/00—Suspension arrangements for wings
    • E05D15/40—Suspension arrangements for wings supported on arms movable in vertical planes
    • E05D15/46—Suspension arrangements for wings supported on arms movable in vertical planes with two pairs of pivoted arms
    • E05D15/466—Suspension arrangements for wings supported on arms movable in vertical planes with two pairs of pivoted arms specially adapted for windows
    • E—FIXED CONSTRUCTIONS
    • E05—LOCKS; KEYS; WINDOW OR DOOR FITTINGS; SAFES
    • E05D—HINGES OR SUSPENSION DEVICES FOR DOORS, WINDOWS OR WINGS
    • E05D3/00—Hinges with pins
    • E05D3/06—Hinges with pins with two or more pins
    • E05D3/14—Hinges with pins with two or more pins with four parallel pins and two arms
    • E—FIXED CONSTRUCTIONS
    • E05—LOCKS; KEYS; WINDOW OR DOOR FITTINGS; SAFES
    • E05Y—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES E05D AND E05F, RELATING TO CONSTRUCTION ELEMENTS, ELECTRIC CONTROL, POWER SUPPLY, POWER SIGNAL OR TRANSMISSION, USER INTERFACES, MOUNTING OR COUPLING, DETAILS, ACCESSORIES, AUXILIARY OPERATIONS NOT OTHERWISE PROVIDED FOR, APPLICATION THEREOF
    • E05Y2900/00—Application of doors, windows, wings or fittings thereof
    • E05Y2900/10—Application of doors, windows, wings or fittings thereof for buildings or parts thereof
    • E05Y2900/13—Type of wing
    • E05Y2900/148—Windows
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/72—Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705
    • G03C1/73—Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705 containing organic compounds
    • G03C1/732—Leuco dyes
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
    • Y10S430/1053—Imaging affecting physical property or radiation sensitive material, or producing nonplanar or printing surface - process, composition, or product: radiation sensitive composition or product or process of making binder containing
    • Y10S430/1055—Radiation sensitive composition or product or process of making
    • Y10S430/127—Spectral sensitizer containing
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
    • Y10S430/163—Radiation-chromic compound

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
  • Materials For Photolithography (AREA)
  • Heat Sensitive Colour Forming Recording (AREA)
  • Printing Plates And Materials Therefor (AREA)
  • Polymerisation Methods In General (AREA)
  • Photosensitive Polymer And Photoresist Processing (AREA)
  • Thermal Transfer Or Thermal Recording In General (AREA)

Abstract

Imaging compositions and methods of using the compositions are disclosed. The imaging compositions are sensitive to low levels of energy such that upon application of the low levels of energy the compositions change color or shade. The compositions may be applied to a work piece to mark it.

Description

Image forming composition and method
Background technology
The present invention relates to image forming composition and method.Can produce the image forming composition and the method for color or tonal variation when more particularly, the present invention relates to be exposed to the low-power energy.
In different industry, adopted many compositions and method to come on base material, to form image, so that this base material of mark (mark).Only give some instances, these industry comprise paper industry, packaging industry, coatings industry, medical industries, dentistry industry, electronics industry, textile industry, aviation and navigation and auto industry and visual art.Usually identify the commodity for example title or the sign of producer with imaging method or labelling method, series number or lot number, fabric type perhaps can made semiconductor wafer with it, and the aviation airship is used for when navigation ship and land vehicle aiming at.
Also usage flag method in Protection Product, photoresist, welding mask, printed panel and other photopolymer product.For example, United States Patent (USP) 5744280 discloses a kind of Photoimageable composition, can form monochrome or multicolor image according to stating, and it has the character of high-contrast image.Described Photoimageable composition comprises photooxidant, photosensitizer, and photic compound and the deuterium of deactivating is for leuco compound.These leuco compound are amino triaryl methine compound or relevant compound, and wherein the degree of the deuterium institute deuterate that methane (center) carbon atom is impregnated in is at least 60%.This patent declares that this deuterium can provide the contrast image of enhancing with respect to corresponding hydrogenation leuco compound for leuco compound.When making Photoimageable composition be exposed to actinic radiation, cause phototropism (phototropic) response.
Label information on label is provided with sign on fabric, perhaps print such information of Business Name for example, series number or other for example lot number or the such information of die location and can be subjected to the directly influence of printing on semiconductor devices.Can adopt stamped method or silk screen print method to print.Because liner has elasticity, so have can be in the advantage of curved surface printing for stamped method, but form aspect the fine pattern unfavorable.Because the female size of the sieve of screen cloth is limited, serigraphy is experience difficulties aspect the acquisition fine pattern also.Except relatively poor degree of accuracy, because printing need be made a plate for each required pattern, perhaps need the time that printing condition is set, so these methods can not be applicable to the occasion that need handle in real time.
Therefore, typographic(al) mark method is replaced by the ink-jet labelling method recently.Although the requirement (this is that many traditional print systems are not available) that the ink-jet labelling method satisfies speed and handles in real time, employed printing ink (it sprays from nozzle under the pressurized condition) has strict regulation.Unless satisfy this strict regulations, otherwise printing ink causes spray nozzle clogging sometimes, causes the increase of reject rate.
In order to overcome this problem, laser border notation has caused attention recently as a kind of high speed and highly efficient labeling method, and comes into operation in some industry.Many laser labelling technical requirements are only to zone laser radiation necessary on the base material, so that irradiated area sex change or remove irradiated area, perhaps base material laser radiation to applying, to remove the coating that is subjected to photograph, between irradiated area (marked region) and non-irradiated area (background), produce contrast thus.
Use laser come mark for example the such goods of semi-conductor chip are a kind of quick and economic labeling methods.Yet, also have some and the relevant shortcoming of the state of the art of laser labelling technology (burn surface to obtain required mark).For example, the mark of laser burn surface gained may be visible at some selected incident angles only to light source.In addition, be deposited on the oil of product surface or other pollutant behind the mark and can besmirch even cover laser labelling.In addition, because the surface that in fact laser want the calcination workpiece, for bare mould mark, relevant calcination may destroy fabric or internal circuit, the internal mold temperature is increased to exceeds the limit that can receive.In addition, when the parts of making are not when being made by the laser active material, the laser active coating that is applied to assembly surface has increased expense, and needs the time to solidify.
Selectively, can use laser-projector with image projection to the surface.They are used on working surface the workpiece location.Some systems have been designed, so that three-dimensional image is projected on embossment shape face rather than the plane.The image of institute's projection is as the model that manufactures a product, and on the layer that is used for the image scanning on the ideal position of certain one deck (ply) is formerly placed.The example of these purposes is to be used for making leather and fur products, the framework on roof and airframe.Laser-projector also is used for locating template or coating mask in the painting process of aircraft.
The position (be used to hole, form the profile of paint sign or picture or arrange the parts of navigation ship so that gluing) of using the laser image of scanning can point out to place or arrange workpiece need have fabulous degree of accuracy during with respect to the position of finished surface at the calibration laser projector.Generally, need six reference point in order enough accurately to calibrate workpiece component.Reverberator or sensor have placed usually near the zone that will place described layer.Because these are in fixing position with respect to workpiece and laser, also will know the position of laser with respect to workpiece.Usually, workman's usage flag or indicia band are carried out manual markings in the position of laser beam image contact workpiece, to limit laser image.This method is too slow, and workman's hand can stop laser image and the aiming at of break beam and workpiece.Thereby, mis-alignment may appear.
Another problem relevant with the laser labelling method is the potential infringement to workman's eyesight.The many laser that use in the mark can make workman's retina damage.Usually, the energy of generation surpasses the laser of 5mW to the dangerous property of workman.
Therefore, be necessary to improve the composition and the method for imaging of mark workpieces of being used for.
Summary of the invention
Image forming composition comprises one or more emulsion, and the amount of described emulsion is enough to influence the color or the tonal variation of (affect) this image forming composition when applying power and be 5mW or littler energy.
In another embodiment, this image forming composition comprises one or more emulsion, the amount of described emulsion is enough to influence the color or the tonal variation of this image forming composition when applying power and be 5mW or littler energy, and one or more short stick or bonding agents.
In another embodiment, this image forming composition comprises one or more emulsion, the amount of described emulsion is enough to influence the color or the tonal variation of this image forming composition when applying power and be 5mW or littler energy, also comprises the composition that forms coating (paint) preparation.
Except one or more emulsion, this image forming composition can comprise one or more binder polymers, plastifier, flowing activity agent, chain-transferring agent, organic acid, surfactant, thickening agent, rheology modifier, thinning agent and other optional member are used for specific markers method and workpiece with the modulation said composition.Said composition can be applied to then on the workpiece to form image, be used to manufacture a product.
Formation method comprises provides a kind of image forming composition, said composition comprises one or more emulsion, the amount of described emulsion is enough to influence the color or the tonal variation of this image forming composition when applying power and be 5mW or littler energy, and said composition is applied on the workpiece; And this image forming composition is applied power is 5mW or littler energy, to influence color or tonal variation.Perhaps, optionally apply energy, on workpiece, to form pattern.Color or tonal variation can be used for making or repairing workpiece, to change the primitive color or the tone of workpiece, perhaps change the color or the tone of workpiece when time in the energy that is exposed to appropriate level.This image forming composition and method provide a kind of and fast and effective method are used for changing the color or the tone of workpiece, perhaps are used at for example aviation airship, on the such workpiece of navigation ship and land vehicle image are set, and perhaps are used for forming on fabric image.
Before workpiece is further handled or afterwards, the part that can remove this image forming composition with appropriate developer or remover (tripper).In addition, because said composition can comprise one or more short stick or bonding agents, therefore undesired part can peel off from workpiece.
This image can be with marking or indicating, for example, for fastener boring so that each several part is linked together, perhaps, perhaps be used for aiming at each parts of navigation ship for making sign aboard or picture forms profile.Because said composition can promptly be applied on the workpiece, and can be that 5mW or littler energy promptly form image by applying power, to produce the contrast of color or tone, therefore the workman no longer need come mark laser beam image with portable mark device or belt near workpiece when making goods.Thereby, because of moving when covering laser beam and using portable mark device or belt to apply mark by the workman, eliminated with the problem of tedious process at a slow speed in workman's hand, perhaps reduced the possibility that the workman is caused eye injury at least.
The minimizing of mistake makes the degree of accuracy of mark be improved.This is important with markers align aviation airship for example during each parts of navigation ship and land vehicle, and the degree of accuracy of these occasion manufacturings is vital for the reliable and safe operation of machine.
Can brush by for example spraying, roller coat, ink-jet, dip-coating, perhaps other suitable method is applied to this image forming composition on the base material.Can apply sufficient energy and include but not limited to laser instrument, infrared and ultraviolet light generating device with the energy source that produces color or tonal variation.Can use conventional device, thereby might not need newly to use described Compounds and methods for special device.In addition, independent, the non-selective cloth said composition of removing on workpiece apply energy rapidly afterwards to produce color or tonal variation, and this makes said composition be suitable for assembly line (assembly line) and goes up use.Thereby said composition provides more efficient manufacture method than the aligning and the imaging processing of many routines.
The accompanying drawing summary
This patent file comprises a painted figure at least.If desired and pay necessary fee, the copy that this patent has color drawings can be provided by Patent Office.
Fig. 1 is the photo in photofading (photofugitive) response of image forming composition dry on the polymer film after selectivity applies laser beam; With
Fig. 2 is the photo in the phototropism response of image forming composition dry on the polymer film after selectivity applies laser beam.
Detailed Description Of The Invention
Use as this specification, unless point out in addition in the literary composition, following meaning is represented in following abbreviation: ℃=degree centigrade; The IR=infrared ray; The UV=ultraviolet ray; The gm=gram; The mg=milligram; The L=liter; The mL=milliliter; The wt%=percentage by weight; Erg=1 dyne centimetre (dyne cm)=10 -7Joule; The J=joule; The mJ=milli is burnt; Nm=nanometer=10 -9Rice; Cm=centimetre; The mm=millimeter; W=watt=erg-ten/second; And mW=milliwatt; Ns=nanosecond; μ sec=microsecond; The Hz=hertz; The KV=kilovolt.
Term " polymer " " and " multipolymer " can exchange use in this specification." actinic radiation " refers to the radiation from the light that can produce chemical change." photofading response (photofugitiveresponse) " refers to applying of energy and causes colored materials to fade or shoal." phototropism response (phototropic response) " refers to applying of energy and causes material deepening (darken)." changing tone (changing shade) " refers to and fades or blackening." (methyl) acrylate " comprises methacrylate and acrylate, and " (methyl) acrylic acid " comprises methacrylic acid and acrylic acid." thinning agent " refers to carrier or medium, for example solvent or solid filling.
Unless point out in addition, all number percent all is meant weight and based on dry weight or solvent-free weight.All numerical ranges all comprise and can any order combinations, are 100% except logically limiting these numerical range summations.
Image forming composition comprises one or more emulsion, and the amount of described emulsion is enough to influence color or tonal variation when applying power 5mW or littler energy.Image forming composition can be applied on the workpiece,,, perhaps on workpiece, be formed into the pattern of picture to influence color or the tonal variation on the whole work-piece with after-applied power 5mW or littler energy.For example, image forming composition optionally can be applied on the workpiece, with after-applied energy influencing color or tonal variation, thereby on workpiece, produce the pattern of imaging.Perhaps, image forming composition can cover on the whole work-piece, optionally applies energy, influencing color or tonal variation, thereby is formed into the pattern of picture on workpiece.
Can image forming composition be applied on the workpiece by the following any suitable method that will discuss.Can remove composition by peel off undesired part from workpiece, perhaps can use appropriate developer or stripper to remove composition.Such developer or remover can be conventional water base or organic developer and removers.
The emulsion that is adopted in said composition is such compound, and it can be by energy activated and change color or tone, perhaps produces one or more other compound and change color or tone when activating.Image forming composition comprises one or more photosensitizers to the visible light sensitivity (photosensitizer), and can be activated by 5mW or littler energy by power.Usually, the content of such emulsion is the 0.005wt% to 10wt% of image forming composition weight, perhaps for example from 0.05wt% to 5wt%, perhaps for example from 0.1wt% to 1wt%.
The activation wavelength of the emulsion that activates in visible-range (sensitizer) is generally greater than 300nm extremely less than 600nm, perhaps for example from 350nm to 550nm, perhaps for example from 400nm to 535nm.This emulsion comprises, but being not limited to cyclopentanone conjugated compound for example 2,5-is two-[4-(lignocaine) phenyl] methylene]-cyclopentanone, 2,5-two [(2,3,6,7-tetrahydrochysene-1H, 5H-benzo (i, j) methylene quinolizine-9-yl)]-cyclopentanone, 2,5-pair-[4-(diethyl-amino)-2-aminomethyl phenyl] methylene]-cyclopentanone.These cyclopentanone can be made by method known in the art by cyclic ketone and tricyclic amino aldehyde.
The example of this suitable conjugate ring pentanone satisfies following chemical formula:
Figure A20051006564300091
Wherein p and q are 0 or 1 independently, and r is 2 or 3; R 1Be hydrogen independently, straight chain or side chain (C 1-C 10) aliphatic group, perhaps straight chain or side chain (C 1-C 10) alkoxy, R 1Usually be hydrogen independently, methyl or methoxyl; R 2Be hydrogen independently, straight chain or side chain (C 1-C 10) aliphatic group, (C 5-C 7) ring (for example alicyclic ring), alkaryl, phenyl, straight chain or side chain (C 1-C 10) hydroxyalkyl, the ether of straight chain or branched hydroxy group end-blocking, for example-(CH 2) v-O-(CHR 3) w-OH, wherein V is from 2 to 4 integer, w is from 1 to 4 integer, R 3Be hydrogen or methyl, perhaps each R 2Carbon atom can form 5 to 7 yuan of having nitrogen together and contain azo-cycle, perhaps one has nitrogen and has and is selected from oxygen, 5 to 7 yuan of second heteroatom of sulphur and second nitrogen contain azo-cycle.This emulsion can activate under 5mW or littler power.
Other emulsion that activates in visible-range includes but not limited to N-alkylamino aryl ketones for example two (9-julolidine groups ketone), and is two-(N-ethyl-1,2,3,4-tetrahydrochysene-6-quinolyl) ketone and p-methoxyphenyl-(N-ethyl-1,2,3,4-tetrahydrochysene-6-quinolyl) ketone; The visible absorption dyestuff that makes in the condensation reaction of base catalysis by aldehyde or two methines, half cyanine and corresponding ketone; Visible absorption squarylium compound; 1,3-dihydro-1-oxo-2H-indene derivative; Any Coumarins dyestuff is ketone group cumarin (ketocoumarin) for example, and 3,3 '-carbonyl two (7-diethyl amino coumarin); For example two (η 5-2,4-cyclopentadiene-1-yl)-two (2,6-two fluoro-3-(1H-pyrroles-1-yl)-phenyl) of halo two cyclopentadiene titanium compounds titanium; And by aryl ketones and compound that two alkyl amino aryl aldehyde are derived and obtained.The example of other emulsion comprises the dyestuff of fluorescein type and based on the light absorber material of triarylmethane nuclear ring (nucleus).These compounds comprise eosin (Eosin), eosin B and rose-red (Rose Bengal).Suitable compound is an Erythrosin B in addition.The method of making this emulsion is being known in the art, and many business methods can be used.Typically, the emulsion that this visible light activates accounts for the 0.05wt% to 2wt% of said composition weight, perhaps 0.25wt% to 1wt% for example, perhaps 0.1wt% to 0.5wt% for example.
Alternatively, this image forming composition can comprise one or more photosensitizers by the UV photoactivation.This emulsion by the UV photoactivation activate wavelength usually from greater than 10nm to less than 300nm, perhaps for example from 50nm to 250nm, perhaps for example from 100nm to 200nm.The emulsion that this UV activates includes but not limited to the polymerization emulsion of weight-average molecular weight from 10000 to 300000,1-[4-(dimethylamino) phenyl for example]-1-(4-methoxyphenyl)-ketone (methanone), 1-[4-(dimethylamino) phenyl]-1-(4-hydroxyphenyl)-ketone and 1-[4-(dimethylamino) phenyl]-1-[4-(2-hydroxyl-oxethyl)-phenyl]-polymkeric substance of ketone; The free alkali dyestuff of ketimide; The aminoderivative dyestuff of triarylmethane; The aminoderivative dyestuff of xanthene; The aminoderivative dyestuff of acridine; Methine dyes; With poly-methine dyes.The method for preparing this compound is known in this area.Usually, this UV activates the 0.05wt% to 1wt% that emulsion accounts for said composition weight, perhaps 0.1wt% to 0.5wt% for example.
Alternatively, this image forming composition can comprise that one or more can be by the photosensitizer of IR photoactivation.This can being generally by the activation wavelength of the emulsion of IR photoactivation greater than 600nm to less than 1000nm, perhaps for example from 700nm to 900nm, perhaps for example from 750nm to 850nm.This IR activates emulsion and includes but not limited to infrared squarylium dyestuff and carbonyl cyanine dye.This dyestuff is known in this area and can be made by the method described in the literary composition.Typically, this dyestuff accounts for the 0.05wt% to 3wt% of said composition weight, perhaps 0.5wt% to 2wt% for example, perhaps 0.1wt% to 1wt% for example.
In this image forming composition, can also use reductive agent.The compound that can be used as reductive agent includes but not limited to one or more naphtoquinone compounds, pyrene quinone for example, for example 1,6-pyrene quinone and 1,8-pyrene quinone; 9,10-anthraquinone, 1-chloroanthraquinone, 2-chloro-anthraquinone, 2-methylanthraquinone, 2-EAQ, 2-tert-butyl group anthraquinone, prestox anthraquinone, 1,4-naphthoquinones, 9,10-phenanthrenequione, 1, and 2-benzo anthraquinone (1,2-benzaanthrquinone), 2,3-benzo anthraquinone, 2-methyl isophthalic acid, 4-naphthoquinones, 2,3-dichloro-naphthoquinones, 1,4-dimethyl anthraquinone, 2,3-dimethyl anthraquinone,, anthraquinone α-sulfonate sodium, 3-chloro-2-methylanthraquinone, the retene quinone, 7,8,9,10-tetrahydrochysene naphtho naphthoquinone and 1,2,3,4-tetrahydrobenzene (methylene) basic anthracene-7,12-diketone.
Other compound that can be used as reductive agent includes but not limited to have the triethanolamine acyl ester of following chemical formula:
N(CH 2CH 2OC(O)-R) 3 (II)
Wherein R is the alkyl with 1 to 4 carbon atom, 0 to 99% nitrilotriacetic acid(NTA) or 3,3 ', 3 "-C of nitrilo-three propionic acid 1-C 4Arrcostab.The example of the acyl ester of this triethanolamine is triethanolamine triacetate and dibenzyl monoethanolamine acetic acid esters.
In image forming composition, can use one or more reductive agents, so that color or the tonal variation of wanting to be provided.Typically, one or more quinones can use with the acyl ester of one or more triethanolamines, so that the reductive agent of wanting function to be provided.The reductive agent deal that is used for composition is 0.05wt% to 50wt%, perhaps 5wt% to 40wt% for example, perhaps 20wt% to 35wt% for example.
Suitable colour former includes but not limited to leuco compound.This leuco compound include but not limited to aminotriaryl methanes, amino xanthene, amino thioxanthene (aminothioxanthene), amino-9, the 10-acridan, amino phenoxazine, aminothiophene piperazine, amino dihydrophenazine, ADP base methine methine (antimodiphenylmethine), colourless indamines, amino hydrocinnamic acid be cyano group ethane and colourless methine for example, hydrazine, colourless indigo dye, amino-2,3-dihydro-anthraquinone, four halogen-p, p '-biphenyl, 2 (p-hydroxybenzene)-4,5-diphenylimidazolidin-4-one and phenethyl aniline.This compound accounts for the 0.1wt% to 5wt% of said composition weight, perhaps 0.25wt% to 3wt% for example, perhaps 0.5wt% to 2wt% for example.
In this image forming composition, can also comprise oxygenant, to influence color or tonal variation.This oxygenant is used in combination with one or more colour formers usually.The compound that can be used as oxygenant includes but not limited to hexa-aryl bi-imidazole compound for example 2,4,5,2 ', the two imidazoles of 4 ', 5 '-hexaphenyl, 2,2 ' 5-three (2-chlorphenyl)-4-(3, the 4-Dimethoxyphenyl)-4,5-diphenyl diimidazole (and isomeride), 2,2 '-two (2-ethoxyphenyls)-4,4 ' 5,5 ' ,-tetraphenyl-1,1 '-two-1H-imidazoles and 2,2 '-two-1-Nai Ji-4,4 ', 5,5 '-tetraphenyl-1 '-two-1H-imidazoles.Other suitable compound includes but not limited to halogenated compound, and described halogenated compound has the key resolution that is not less than 40 kilocalories every mole, and producing first halogen as free radical, and hydrogen on it attached thereto is no more than 1; Sulfuryl halide with following general formula: R '-SO 2-X, wherein R ' is an alkyl, thiazolinyl, naphthenic base, aryl, alkaryl, perhaps aralkyl, X is chlorine or bromine; Sulfinyl sulfide with following general formula: R "-S-X ', wherein R " and X ' have and top R ' and the same implication of X; Four aryl hydrazines, benzothiazole based bisulfide, poly-methyl aryl aldehyde, alkylidene 2,5-cyclohexadiene-1-ketone, azobenzyl (azobenzyl), nitroso-, alkyl (T1), superoxide, and halogenated amine.The deal of included this compound accounts for the 0.25wt% to 10wt% of said composition weight in the said composition, perhaps 0.5wt% to 5wt% for example, perhaps 1wt% to 3wt% for example.The method for preparing this compound is that known and many business methods can adopt in this area.
In this image forming composition, can comprise the bonding agent that film forming polymer is used as composition.Film forming polymer in the preparation of these compositions, can adopt any binder for film formation, as long as can not produce adverse influence to color or the tonal variation of wanting.The deal of included film forming polymer accounts for the 10wt% to 90wt% of composition weight, perhaps 15wt% to 70wt% for example, perhaps 25wt% to 60wt% for example.Typically, film forming polymer is obtained by acid functional monomer and non-acid functional monomer's potpourri.Sour and non-acid functional monomer is combined together to form multipolymer, makes acid number from least 80, perhaps for example in from 150 to 250 scopes.Suitable acid functional monomer's example comprises (methyl) acrylic acid, maleic acid, fumaric acid, citraconic acid, 2-propenyl amino (acrylamino)-2-methyl propane sulfonic acid, phosphoric acid 2-hydroxyethyl propylene alcohol ester, phosphoric acid 2-hydroxypropyl propylene alcohol ester and phosphoric acid 2-hydroxyl-α-propylene alcohol ester.
Suitable non-acid functional monomer's example comprises for example methyl acrylate of (methyl) acrylic acid ester, 2-EHA, the just own ester of n-butyl acrylate, acrylic acid, methyl methacrylate, Hydroxyethyl Acrylate, butyl methacrylate, 2-ethyl hexyl acrylate, methacrylic acid 2-ethoxy ethyl ester, tert-butyl acrylate, 1,5 pentandiol diacrylate, N, N-diethylamino ethyl propylene acid esters, ethylene glycol diacrylate, diacrylate 1, ammediol ester, diacrylate decanediol ester, dimethacrylate decanediol ester, diacrylate 1,4-cyclohexanediol ester, 2,2-dihydroxy methylpropane diacrylate, diacrylate glycerine ester, diacrylate tripropylene glycol ester, three acrylic acid glycerine esters, 2,2-two (to hydroxyphenyl)-propane dimethylacrylate, diacrylate triglycol ester, polyoxy ethyl-2,2-two (to hydroxyphenyl)-propane dimethylacrylate, dimethacrylate triglycol ester, polyoxyethyl propyl trimethylolpropane triacrylate, Ethylene glycol dimethacrylate, tetramethylene dimethacrylate, dimethacrylate 1, ammediol ester, trimethyl acrylic acid 1,2,4-butantriol ester, 2,2,4-trimethyl-1,3-pentanediol dimethylacrylate, pentaerythritol acrylate trimethyl, 1-phenyl ethene-1, the 2-dimethylacrylate, pentaerythrite tetramethyl acrylate, trimethylol-propane trimethacrylate, dimethacrylate 1, the 5-pentadiol ester; Styrene and substituted phenylethylene be for example vinyl acrylate and metering system vinyl acetate of 2-methyl styrene and vinyltoluene and vinyl acetate for example.
Other suitable polymers includes but not limited to for example polyvinyl alcohol (PVA) of non-ionic polymers, polyvinyl pyrrolidone, hydroxyl-ethyl cellulose and hydroxyethyl propyl methocel.
In this image forming composition, can use chain-transferring agent.This chain-transferring agent is as accelerator.In this image forming composition, can use one or more chain-transferring agents.Chain-transferring agent or accelerator have increased the speed that is exposed to color after the energy or tonal variation.The compound of any acceleration color or tonal variation can use.The deal that is included in the accelerator in the said composition can be 0.01wt% to 25wt%, perhaps 0.5wt% to 10wt% for example.The example of suitable accelerator comprises salt and amine.
Suitable salt includes but not limited to that wherein kation is the salt of iodine or sulfonium, the salt Phosphonium (phosphonium) of aryl-sulfonyl oxygen benzene sulphur sulfonate anionic for example, oxo sulfoxonium (oxysulfoxonium), sulfoxonium (sulfoxonium), ammonium, diazonium (diazonium), selenium (selononium), arsine (arsonium), replace the N-heterocyclic radical with N-, wherein N is by replacing or unsubstituted saturated or undersaturated alkyl or aryl are replaced.
The negative ion of salt can be a chloride or non-nucleophilicity negative ion tetrafluoroborate for example for example, hexafluoro-phosphate radical, the hexafluoro arsenate, hexafluoro metaantimmonic acid root, trifluoromethanesulfonic acid root (triflate), four-(five fluorophosphoric acid roots) borates, five fluorinated ethylene sulfonate radicals, to the methyl-benzyl sulfonate radical, ethylsulfonic acid root, trifluoromethyl acetate and pentafluoroethyl group acetate.
The example of typical salt comprises for example chloro diphenyl iodine, diphenyl iodine hexafluorophosphate, diphenyl iodine hexafluoro antimonate, chlorination 4,4-dicumyl iodine, dicumyl iodine hexafluorophosphate, N-methoxyl-a-picoline-tosilate, 4-methoxybenzene-diazonium tetrafluoroborate, 4,4 '-two dodecyl benzene iodo-hexafluorophosphates, chlorination 2-cyanoethyl triphenyl phosphonium, two-(4-diphenyl sulfonium (sulfonion) phenyl) sulfide-two-hexafluorophosphate, two-4-dodecyl benzene iodine hexafluoro antimonate and triphenylsulfonium hexafluoro antimonate.
Suitable amine includes but not limited to primary amine, and secondary amine and tertiary amine be methylamine for example, diethylamine, and triethylamine, heterocyclic amine be pyridine and piperidines for example, and aromatic amine is aniline for example, and quaternary ammonium halide is for example fluoridized for example tetraethyl ammonium hydroxide of tetraethyl amine and quaternary ammonium hydroxide.Triethanolamine among the general formula I I also has the accelerator activity.
In said composition, can also comprise plastifier.Can adopt any suitable manufacturing methods.The deal of included plastifier can account for the 0.5wt% to 15wt% of said composition weight, perhaps 1wt% to 10wt% for example.The example of suitable manufacturing methods comprises for example dibutyl phthalate of phthalic ester; dibutyl phthalate (DHP); dioctyl phthalate and diallyl phthalate; glycol is polyglycol and polypropylene glycol for example; diol ester is triethylene glycol diacetate for example; four ethylidene glycol diacetates and dipropylidene diol dibenzoate, phosphate is tricresyl phosphate for example; triphenyl phosphate; acid amides is para toluene sulfonamide for example, benzsulfamide, N-normal-butyl acetone amine (acetoneamide); fatty group dibasic acid is diisobutyl-adipate for example; the dioctyl adipate, dimethyl sebacate, dioctyl azelate; the dibutyl malate; triethyl citrate, three normal-butyl acetyl group citrates, butyl-laurate; dioctyl-4; 5-diepoxy cyclohexane-1,2-dicarboxylic ester and glycerine triacetyl ester.
In said composition, can comprise one or more flowing activity agent.The flowing activity agent is the compound that level and smooth and smooth coating are provided on base material.The deal of included flowing activity agent can account for the 0.05wt% to 5wt% of composition, perhaps 0.1wt% to 2wt% for example.Suitable flowing activity agent includes but not limited to the multipolymer of alkyl acrylate.A multipolymer that example is ethyl acrylate and 2-EHA of this alkyl acrylate.
Alternatively, in image forming composition, can adopt one or more organic acids.The organic acid consumption can be 0.01wt% to 5wt%, perhaps 0.5wt% to 2wt% for example.The example of appropriate organic comprises formic acid, acetate, propionic acid, butyric acid, valeric acid, caproic acid, sad, turn sour, lauric acid, phenylacetic acid, benzoic acid, phthalic acid, m-phthalic acid, terephthalic acid (TPA), hexane diacid, 2 ethyl hexanoic acid, isobutyric acid, 2-Methyl Butyric Acid, 2-propylheptanoic acid, the 2-phenylpropionic acid, 2-(to isobutylphenyl) propionic acid, and 2-(6-methoxyl-2-naphthyl) propionic acid.
Alternatively, in image forming composition, can use one or more surfactants.The deal that is included in the surfactant in the said composition can account for the 0.5wt% to 10wt% of said composition, perhaps 1wt% to 5wt% for example.Suitable surfactant comprises nonionic, ion and amphoteric surfactant.The example of suitable non-ionic surfactant comprises polyethylene oxide ether, the derivant of polyethylene oxide, fragrant ethoxylate, the segmented copolymer of acetylene series (acetylenic) oxirane and oxirane and epoxypropane.The example of suitable ionic surface active agent comprises alkali metal salt, alkali salt, ammonium salt and the alkanol ammonium salts of alkyl sodium sulfate ester, alkyl sodium sulfate ethoxylated ester and benzene sulfonic acid Arrcostab.The example of suitable amphoteric surfactant comprises the derivant of secondary aliphatic amine and tertiary amine; wherein fat-based can be straight chain or side chain; and one of them or fatty substituting group comprise 8 to 18 carbon atoms; one comprises for example carboxyl of anionic water-soluble group; sulfo group; sulfato, phosphate, phosphono.The concrete example of this amphoteric surfactant is 3-sodium dodecyl aminopropionitrile and 3-dodecyl amino propane sulfonic acid sodium.
The thickening agent that in this image forming composition, can comprise common deal.In this image forming composition, can introduce any suitable thickening.Typically, thickening agent accounts for the 0.05wt% to 10wt% of said composition weight, perhaps for example in 1wt% to the 5wt% scope.Can adopt conventional thickening agent.The example of suitable thickening comprises that low molecular weight polyurethane for example has three hydrophobic groups at least, and described hydrophobic group is by the interconnection of polyethers hydrophilic group.The molecular weight of this thickening agent is in 10,000 to 200,000 scopes.Other suitable thickening comprises the alkali soluble emulsion of hydrophobically modified, the hydroxyethyl cellulose of hydrophobically modified and hydrophobic modified polyacrylamide.
The rheology modifier that can comprise routine dose.Typically, the consumption of rheology modifier accounts for the 0.5wt% to 20wt% of said composition weight, perhaps 5wt% to 15wt% for example.The example of rheology modifier comprises vinyl aromatic polymers and acrylic polymers.
In this image forming composition, can comprise thinning agent, think that other composition provides media or carrier.Thinning agent adds as required.The addition of solid diluent or filling material makes that usually the dry weight of said composition is 100wt%.The example of solid diluent is a cellulose.Use liquid diluent or solvent to be used for making solution, suspending liquid, dispersion liquid or the emulsifying agent of said composition active component.This solvent can be water-based or organic, perhaps their potpourri.Representative examples of organic comprises for example methyl alcohol of alcohol, ethanol and isopropyl alcohol, diisopropyl ether, diethylene glycol dimethyl ether, 1,4-diox, tetrahydrofuran or 1,2-dimethoxy propane, with ester butyrolactone for example, ethylene carbonate ester and propylene glycol carbonate, ether-ether such as acetic acid methoxyl ethyl ester, ethoxyethyl acetate(EA), 1-methoxy-propyl 2-acetic acid esters, 2-methoxy-propyl-1-acetic acid esters, 1-ethoxycarbonyl propyl-2-acetic acid esters and 2-ethoxycarbonyl propyl-1-acetic acid esters, ketone is acetone and methyl ethyl ketone for example, nitrile is acetonitrile for example, and propionitrile and methoxypropionitrile, sulfone be sulfolane (sulfolan) for example, two first sulfones and two second sulfone and phosphate be trimethyl phosphate and triethyl phosphate for example.
This image forming composition can be the form of concentrate.In this concentrate, the content of solid matter perhaps for example accounts for 85wt% to 95wt% for accounting for 80wt% to 98wt%.Concentrate can water, one or more organic solvents, the perhaps mixture diluted of water and one or more organic solvents.The dilution of concentrate makes solid matter content account for 5wt% to less than 80wt%, perhaps for example 10wt% to 70wt%, perhaps for example 20wt% to 60wt%.
In this image forming composition, can comprise adhesion promotor, to improve the adhesion between this image forming composition and the workpiece.Can use any suitable adhesion promotor.The deal of included this adhesion promotor can account for the 0.5wt% of said composition weight to 10wt%, perhaps for example 1wt% to 5wt%.The example of this adhesion promotor comprises acrylamido glycolic acid (moisture with anhydrous), two propylene acylamino-acetate, 3-acrylamido 3-methyl-butyric acid and their potpourri.
Selectable, can be in this image forming composition mixed adhesive so that composition is bonded on the workpiece securely.The example of suitable bonding is a releasable adhesive.Any releasable adhesive can use in this image forming composition, as long as it can disturb color or the tonal variation of wanting sharply.Releasable adhesive makes and can said composition be removed by from base material they being peeled off, and makes and can said composition be removed by appropriate developer or remover.The deal of included releasable adhesive accounts for the 0.05wt% of said composition weight to 10wt%, perhaps 0.1wt% to 5% for example, perhaps for example 1wt% to 3wt%.Suitable releasable adhesive includes but not limited to contact adhesive.The example of this bonding agent comprises acrylic compounds, polyurethane, polyalphaolefin, polysiloxane (silicone), the combination of esters of acrylic acid contact adhesive and thermoplastic elastomer class contact adhesive, and the natural rubber and the ameripol of viscosity enhancing.
The combination of esters of acrylic acid contact adhesive and thermoplastic elastomer class contact adhesive comprise 10wt% to 90wt% or for example 30wt% to the esters of acrylic acid contact adhesive of 70wt%, and 10wt% to 90wt% or for example 30wt% to the elastic body class contact adhesive of 70wt%.The example of suitable esters of acrylic acid contact adhesive can (its polymkeric substance has and is not more than 0 ℃ T by simple function (methyl) acrylate of at least a polymerization g(glass transition temperature)) and the simple function ethylenically unsaturated monomers of optional at least a copolymerization (its homopolymer has at least 10 ℃ T g) obtain.This simple function ethylenically unsaturated monomers may reside in the acrylate component of bonding agent, and its deal accounts for 5wt% to 10wt%.Thermoplastic elastomer class contact adhesive composition can for example the segmented copolymer of styrene and polybutadiene or polyisoprene or their potpourri be formed by the free radical segmented copolymer.Alternatively, can comprise crosslinking chemical.
Can the mixed light sensitive ingredient in this releasable adhesive composition and any other optionally be included in adjuvant in the said composition.Can use conventional method to mix various compositions.Can brush by for example spraying, dipping, roller coat or laminating are applied to said composition on the base material.Can remove any solvent or residual solvent by air drying or from the heat that hot-air drier applies q.s, between said composition and workpiece, to form adhesion.
When this image forming composition was used for coating, this coating comprised for example thickening agent, rheology modifier, and thinning agent and other optionally typically are used for the composition of coating formulation.
These compositions (it has formed this image forming composition) can mix with any suitable method known in the art.These compositions can use conventional device to mix, to form solid mixture, concentrate, solution, suspension, dispersion liquid or emulsion.Preparation process is generally finished in the luminous environment in control, is activated prematurely to prevent in these compositions one or more.Said composition can be stored afterwards,, perhaps after configuration, it is applied on the base material rapidly by above-mentioned arbitrary method so that use later on.Typically, said composition was stored in before using in the control luminous environment.For example, typically, configuration and storage are by the composition of the emulsion that has the visible light activation under ruddiness.
In case image forming composition is applied enough energy, the response of fugitiveness to light or phototropism will occur.The amount of energy can be 0.2mJ/cm 2Perhaps bigger, perhaps 0.2mJ/cm for example 2To 100mJ/cm 2, perhaps 2mJ/cm for example 2To 40mJ/cm 2, perhaps 5mJ/cm for example 2To 30mJ/cm 2
Apply power and be 5mW or still less (also promptly greater than 0mW), perhaps for example from less than 5mW to 0.01mW, perhaps for example from 4mW to 0.05mW, perhaps for example from 3mW to 0.1mW, perhaps for example from 2mW to 0.25mW, perhaps for example during the energy from 1mW to 0.5mW image forming composition color or tonal variation can take place.Typically, such power is produced by the light source in the visible-range.In a single day color or tonal variation can take place when being exposed to from the luminous energy outside the visible light in other photosensitizer and energy-sensitive composition (it can be included in this image forming composition).These included photosensitizers and energy-sensitive compound provide more significant color or tone contrast for 5mW that is applied or the littler caused response of energy.Typically, the phototropism response can take place in this photosensitizer and energy-sensitive compound (photosensitizer is subjected to 5mW or more low power energy activated and form color or tone contrast).
Although in theoretical scope, not it is believed that, wherein relate to one or more colors or tonal variation mechanism, color or tonal variation are provided after applying energy.For example, when causing photofading when response, one or more emulsion discharge free radicals activating one or more reductive agents, thereby have reduced one or more emulsion, thereby also influence color or tonal variation in the said composition.When causing the phototropism response, for example, cause redox reaction between one or more leuco compound and one or more oxygenants, thereby influenced the variation of color or tone from the free radical of one or more emulsion.Some preparations have photofading response and phototropism response simultaneously.For example, it also is in the laser that composition is exposed to artificial energy, produce free radical from one or more emulsion, activate one or more reductive agents then and reduce described emulsion, thereby the photofading response takes place, should be exposed in the surround lighting by same composition then, make one or more one or more leuco compound of oxygenant oxidation.
Can use any appropriate energy source to cause photofading response or phototropism response.The example of appropriate energy source includes but not limited to laser and flashlamp, and laser comprises from hand-held laser and 3-D imaging system and produces laser.The operation wavelength of laser can be from IR to UV.This paper has described the laser of two kinds of classics that are suitable for causing color or tonal variation.
Excimer laser is a kind of superpower laser, and it can produce the high-throughout light in the UV frequency range.Their laser capacity is based on being excited of specific diatomic gas molecule.Particularly, excimer laser constitutes a series of laser instruments, the light of its emission wavelength in 157nm to 355nm scope.Prevailing excitation wavelength and corresponding diatomic gas are XeCl (308nm), KrF (248nm), and ArF (193nm).Continuous action in the excimer laser is the formed result who is excited the particle counter-rotating in the light modulator of diatomic gas.Pulse width is 10ns to 100ns, and this produces the pulse of a high-energy short pulse width.
Solid-state laser is a kind of superpower laser, the gathering light beam in it can produce from IR to the UV wavelength coverage.The selection of these solid-state lasers partly is based on material and requires neodymium is doped to for example yttrium-aluminium garnet (YAG) of solid matrix, yttrium-lithium-fluoride (YLF) and vanadic acid yttrium (YVO 5) in.These materials send the laser of the fundamental wavelength in 1.04 to 1.08 microns the IR scope.By using nonlinear optical crystal for example three lithium borates (LBO) or titanium phosphate potassium (KTP), this laser can expand to more short wavelength, in an example, use such crystal, can be increased to wavelength 532nm from basic 1.06 microns its frequencies of radiation in the YAG laser instrument of doping neodymium.
The example of the excimer laser light source that can replace is the linear excimers of short pulse, the UV flashlamp.This lamp comprises that transparent quartz burner and thick 1mm, an inner aperture are 3 to 20mm wall.This flashlamp can long 30cm.Be sealed to the terminal part of fluorescent tube by the electrode of tungsten manufacturing, it with your gas for example xenon fill.By using the capacitor group, electrode is applied the high voltage of 5KV to the 40KV scope, this flashlamp sends 1Hz to the interior pulse of 20Hz scope.To form plasma, plasma sends wavelength coverage at the wide band radiation of 200nm to 800nm to electric charge with the xenon atom ionization.Flashlamp can comprise that part is placed on this fluorescent tube reverberator on every side, the radiation from lamp is shaped and is directed to mask or workpiece.
Linear flashlamp can produce high power at the wavelength place shorter with respect to the short pulse of 5 μ sec, high-throughout energy output.For example, the broadband spectrum output that has been found that linear xenon flash lamp can provide usefulness at 2 μ sec 1J/cm in the impulse duration of 6 μ sec 2To 1.5J/cm 2Energy density.
By peel off undesired part from base material,, can be from the base material whole or partly remove described image forming composition perhaps by using appropriate developer or remover.Developer and remover can be the classes water class or organic.For example, the solution of conventional water class can be used for removing the image forming composition of the polymer adhesive that wherein has acid official energy.The example of this water class solution is for example sodium carbonate and a solution of potassium carbonate of alkaline metal aqueous solution.The conventional organic developer that is used for removing from workpiece composition includes but not limited to for example benzylamine of primary amine, and butylamine and allylamine, secondary amine be for example trimethylamine and triethylamine of dimethylamine and tertiary amine for example.
This image forming composition provides a kind of and fast and effective method is used to change the color and tint of workpiece, perhaps at workpiece aviation airship for example, places image on navigation ship and the land craft, perhaps is used for forming on fabric image.After being coated with this image forming composition, the energy that applies capacity to this image forming composition to change its color or tone.Usually, the variation of color or tone is stable.The stable meaning is that color or tonal variation continue at least 10 seconds, perhaps for example from 20 minutes to 2 days, perhaps for example from 30 minutes to 1 hour.
Selectively, can optionally apply energy forming the pattern of an imaging, and can further handle workpiece to form last goods.For example; can use this image to get out and be used for fastening boring as mask or indication; so that for example each parts in the automobile assembling link together, perhaps form a profile that is used on airframe, making sign or picture, perhaps aim at each parts of navigation ship.Because said composition can promptly be applied on the workpiece, and can apply energy by selectivity and form image rapidly, contrast to produce color or tone, so the workman no longer need come mark laser beam image near workpiece with portable ink markings device or belt when making goods.Thereby, because of the problem that the workman uses portable mark device and belt to cover laser beam is eliminated.
In addition, the minimizing of mistake makes the degree of accuracy of mark be increased.This is aiming at for example aviation airship with mark, be important during each parts of navigation ship and land vehicle, and the degree of accuracy of these occasion manufacturings is vital for the reliable and safe operation of machine.
Said composition is suitable for the manufacturing of the industry group wiring of many goods.For example, for example the base material of airframe can pass through worktable 1, there said composition is applied to the surface of airframe, with covering want partly or completely the surface.Can said composition be coated on the fuselage by the spraying or the roller coat operation of standard, perhaps brush on its surface.Airframe with coating is sent to worktable 2 then, there its whole surface is applied energy, perhaps optionally applies energy, to form pattern.When first airframe is in worktable 2, second fuselage can be moved on to worktable 1 and be coated with.Can use laser beam to apply energy, it makes the surface of airframe that color or tonal variation take place.Owing to do not need workman's manual markings, the airframe of this imaging can promptly be sent on the worktable 3, is used for further processing, for example develops or peels off undesired coated portion, perhaps on fuselage, be fastener boring, so that on other worktable, aim at each parts.In addition owing to there is not the workman to disturb laser beam to arrive the light path of specified point on the airframe of coating, so on the imaging worktable workman remove the accuracy that has improved imaging.Thereby said composition provides more effective manufacture method than the imaging and the Alignment Process of many routines.In addition, because pattern forms and can use lower powered light source (also being 5mW or littler) to carry out, the danger of workman's eyesight is also eliminated or has been reduced at least.
Embodiment 1
Photofading composition and response thereof
The disclosed composition of following table mixes under 20 ℃, ruddiness, forms a kind of uniform mix.
Table 1
Composition Percentage by weight
The just own ester of methacrylic acid, methymethacrylate, n-butyl acrylate, the multipolymer of styrene and methacrylic acid 55
Dibenzoic acid dipropylene glycol ester 16
Hexaarylbiimidazole 2
9, the 10-phenanthrenequione 0.2
The triethanolamine triacetate 1.5
Colourless (leuco) crystal violet 0.3
2, two [[4-(diethylamino) phenyl] the methylene]-cyclopentanone of 5-, (2E, 5E) 0.1
Methyl ethyl ketone Capacity makes weight of formulation reach 100%
This multipolymer is by the just own ester of 29wt% methacrylic acid, the 29wt% methymethacrylate, and the 15wt% n-butyl acrylate, 5wt% styrene, the methacrylic acid monomer of 22wt% makes.Use the solid mixture of the methyl ethyl ketone formation 45wt% of capacity.This multipolymer adopts conventional Raolical polymerizable to form.
After making this uniform mix, it is sprayed on the polyethylene film.This polyethylene film be 30cm * 30cm and thick be 250 microns.Use hair drier with this uniform mix drying, to remove methyl ethyl ketone.
Under UV light, the dry coating on polyethylene film is rufous as shown in Figure 1.In the time of in this coating optionally being exposed to from the 532nm light of hand-held laser, expose portion fades, and presents the grey shown in four rectangular patterns among Fig. 1.
Embodiment 2
Phototropism response and composition
The listed composition of following table mixes under 20 ℃, UV, forms a kind of uniform mix.
Table 2
Composition Percentage by weight
The just own ester of methacrylic acid, methymethacrylate, n-butyl acrylate, the multipolymer of styrene and methacrylic acid 64
Dibenzoic acid dipropylene glycol ester 19
Bifluoride two luxuriant titaniums 3
Leuco crystal violet 1
Methyl ethyl ketone Capacity makes weight of formulation reach 100%
This multipolymer uses as among the embodiment 1.After making this potpourri, it is sprayed on the polyethylene film under UV light.This polyethylene film be 30cm * 30cm and thick be 250 microns.Use hair drier with this uniform mix drying.Under UV light, this coating is yellow green as shown in Figure 2.
Will from the energy selectivity of the 532nm wavelength of hand-held laser be applied on this coating, four rectangular patterns that form because of the laser deepening have formed four purple rectangles as shown in Figure 2.
Embodiment 3
Photofading response composition with adhesion promotor
Following composition prepares under 20 ℃, ruddiness.
Table 3
Composition Percentage by weight
The just own ester of methacrylic acid, methymethacrylate, n-butyl acrylate, the multipolymer of styrene and methacrylic acid 80
The pyrene quinone 1
The triethanolamine triacetate 1.3
Leuco crystal violet 0.5
The conjugate ring pentanone 0.2
Hexaarylbiimidazole 3
The bisacrylamind guanidine-acetic acid 1
Methyl ethyl ketone Capacity makes weight of formulation reach 100%
The same among this multipolymer and the embodiment 1.Use conventional mixing arrangement to mix these compositions, to form uniform mix.
This uniform mix is rolled onto on the polyethylene terephthalate with the supporting of the bonding agent belt of strippable cellulose peel ply.This bisacrylamind guanidine-acetic acid adhesion promotor improves the clinging power between coating and the releasable bonding agent belt backing.
Optionally apply the laser beam of 532nm, cause the coating of expose portion to become transparent clear from amber.
Embodiment 4
Photofading response composite with bonding agent
Composition below the preparation.
Table 4
Composition Percentage by weight
The just own ester of methacrylic acid, methymethacrylate, n-butyl acrylate, the multipolymer of styrene and methacrylic acid 85
9, the 10-phenanthrenequione 0.5
The triethanolamine triacetate 1.3
Leuco crystal violet 0.5
The conjugate ring pentanone 0.2
Hexaarylbiimidazole 2
The polysiloxane ethylenic copolymer 10
Methyl ethyl ketone Capacity makes weight of formulation reach 100%
This multipolymer is the same with multipolymer among the embodiment 1.Use conventional mixing arrangement to mix these compositions down, to form uniform mix at 20 ℃.In ruddiness, handle this potpourri.
This uniform mix is rolled onto has 40cm * 40cm and thick on the releasable adhesive belt of 5mm polyethylene terephthalate backing.Use conventional electric fan to remove methyl ethyl ketone at 20 ℃.Between this coating and polyethylene terephthalate backing, has good clinging power.
Optionally apply light, cause the selection part of coating to become transparent clear from amber from the 532nm of hand-held laser.
Embodiment 5
Photosensitive composition in the coating formulation
Formulation for coating material below the preparation.
Table 5
Composition Percentage by weight
Tamol TM731 (25%) spreading agents 1
Propylene glycol 2
Patcote TM801 (defoamers) 1
Titania-pure R-900 23
Optiwhite TM(china clay) 9
Attagel TM50 (green thread stone clays) 1
The acrylic acid series polymeric compounds bonding agent 32
Texanol TM 1
The thickening agent aqueous mixtures 21
Water Capacity makes weight of formulation reach 100%
With the formulation for coating material in the disclosed photosensitive composition mixture table 5 of the table 4 of embodiment 4, make this photosensitive composition comprise this end formulation of 5wt%.This coating and this photosensitive composition mix with conventional mixing arrangement down at 20 ℃, to form uniform mix.This potpourri is handled under ruddiness.
This coating/photosensitive composition potpourri is rolled onto 80cm * 80cm and thick on the aluminium sample of 5mm.Between potpourri and aluminium sample, has good clinging power.
Optionally apply light, cause the selection part of coating to become transparent clear from amber from the 532nm of hand-held laser.

Claims (10)

1. an image forming composition comprises one or more emulsion, and the amount of described emulsion is enough to influence the color or the tonal variation of this image forming composition when applying power and be 5mW or littler energy.
2. image forming composition as claimed in claim 1, it also comprises one or more reductive agents, colour former, oxygenant, binder polymer, plastifier, flowing activity agent, chain-transferring agent, organic acid, adhesion promotor, rheology modifier, thickening agent, surfactant, bonding agent and thinning agent.
3. image forming composition as claimed in claim 1 is characterized in that described one or more emulsion are shown in following chemical formula:
Figure A2005100656430002C1
Wherein p and q are 0 or 1 independently, and r is 2 or 3; R 1Be hydrogen, straight chain or side chain (C independently 1-C 10) aliphatic group, perhaps straight chain or side chain (C 1-C 10) alkoxy; R 2Be respectively hydrogen, straight chain or side chain (C 1-C 10) aliphatic group, (C 5-C 7) ring, alkaryl, phenyl, straight chain or side chain (C 1-C 10) ether or each R of hydroxyalkyl, straight chain or branched hydroxy group end-blocking 2Carbon atom can combine and form 5 to 7 yuan the azo-cycle that contains, perhaps form and contain aerobic, sulphur or second nitrogen and contain azo-cycle as second heteroatomic 5 to 7 yuan.
4. image forming composition comprises the conjugation photosensitizer of one or more cyclopentanones, and the amount of described photosensitizer is enough to influence the color or the tonal variation of this image forming composition when applying power and be 5mW or littler energy.
5. image forming composition as claimed in claim 4, it also comprises one or more reductive agents, colour coupler, oxygenant, binder polymer, plastifier, flowing activity agent, chain-transferring agent, organic acid, surfactant, thinning agent, rheology modifier, thickening agent, adhesion promotor and bonding agent.
6. image forming composition as claimed in claim 5 is characterized in that the conjugation photosensitizer of described one or more cyclopentanones accounts for the 0.005wt% of said composition to 10wt%.
7. image forming composition, comprise one or more emulsion, one or more thinning agents, one or more rheology modifiers and one or more thickening agents, the amount of described one or more emulsion is enough to influence the color or the tonal variation of this image forming composition when applying power and be 5mW or littler energy.
8. method comprises:
A) provide a kind of image forming composition, said composition comprises one or more emulsion, and the amount of described emulsion is enough to influence the color or the tonal variation of this image forming composition when applying power and be 5mW or littler energy.
B) said composition is applied on the workpiece; And
C) this image forming composition being applied power is 5mW or littler energy, to influence color or tonal variation.
9. method as claimed in claim 8 is characterized in that the energy that is applied is at least 0.2mJ/cm 2
10. method as claimed in claim 8, wherein with this energy selectivity be applied on this image forming composition, to form pattern.
CN2005100656435A 2004-02-06 2005-02-06 Imaging compositions and methods Expired - Fee Related CN1776522B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US10/773,990 US7270932B2 (en) 2004-02-06 2004-02-06 Imaging composition and method
US10/773,990 2004-02-06

Publications (2)

Publication Number Publication Date
CN1776522A true CN1776522A (en) 2006-05-24
CN1776522B CN1776522B (en) 2012-08-01

Family

ID=34679399

Family Applications (2)

Application Number Title Priority Date Filing Date
CN2005100081457A Expired - Fee Related CN1727996B (en) 2004-02-06 2005-02-06 Improved image forming composition and method
CN2005100656435A Expired - Fee Related CN1776522B (en) 2004-02-06 2005-02-06 Imaging compositions and methods

Family Applications Before (1)

Application Number Title Priority Date Filing Date
CN2005100081457A Expired - Fee Related CN1727996B (en) 2004-02-06 2005-02-06 Improved image forming composition and method

Country Status (6)

Country Link
US (1) US7270932B2 (en)
EP (1) EP1562073A1 (en)
JP (2) JP2005234561A (en)
KR (1) KR101183265B1 (en)
CN (2) CN1727996B (en)
TW (1) TW200602802A (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050175941A1 (en) * 2004-02-06 2005-08-11 Rohm And Hass Electronic Materials, L.L.C. Imaging composition and method
US7977026B2 (en) * 2004-02-06 2011-07-12 Rohm And Haas Electronic Materials Llc Imaging methods
US20070117042A1 (en) * 2005-11-23 2007-05-24 Rohm And Haas Electronic Materials Llc Imaging methods
US8088549B2 (en) * 2007-12-19 2012-01-03 Eastman Kodak Company Radiation-sensitive elements with developability-enhancing compounds
WO2009121055A1 (en) * 2008-03-28 2009-10-01 Georgia Tech Research Corporation Reduced dye probes for the detection of radical oxygen species
CN113165315A (en) * 2018-12-20 2021-07-23 东丽株式会社 Fabric printed matter

Family Cites Families (95)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB544983A (en) 1940-11-25 1942-05-06 Redpath Brown & Company Ltd Improvements relating to the manufacture of constructional work and the production of templates or like marking-off devices
US3630736A (en) * 1962-10-31 1971-12-28 Du Pont Leuco dye/hexaarylbiimidazole compositions and processes
US3445234A (en) * 1962-10-31 1969-05-20 Du Pont Leuco dye/hexaarylbiimidazole imageforming composition
US3390997A (en) * 1964-04-29 1968-07-02 Du Pont Photosensitive composition comprising a triphenylemethane derivative and a nitrogen-containing photo-oxidant
US3598592A (en) * 1967-11-07 1971-08-10 Du Pont Storage-stable photosensitive aminotriarylmethane/selected organic photooxidant compositions
US3666466A (en) * 1969-11-26 1972-05-30 Du Pont Deactivating dual response photosensitive compositions with visible and ultraviolet light
US3652275A (en) * 1970-07-09 1972-03-28 Du Pont HEXAARYLBIIMIDAZOLE BIS (p-DIALKYL-AMINOPHENYL-{60 ,{62 -UNSATURATED) KETONE COMPOSITIONS
US3658543A (en) * 1970-12-18 1972-04-25 Du Pont Dual response photosensitive composition containing acyl ester of triethanolamine
US3761942A (en) * 1971-07-28 1973-09-25 Ibm Low energy thermochromic image recording device
US3977953A (en) * 1972-04-10 1976-08-31 Atlantic Research Institute Ltd. Process for the production of hulupones
US3993489A (en) * 1973-11-14 1976-11-23 Monsanto Company Multi-color laminate of photopolymer that is image-wise hydroperoxidized
US4155892A (en) * 1975-10-03 1979-05-22 Rohm And Haas Company Polyurethane thickeners for aqueous compositions
JPS5265425A (en) * 1975-11-24 1977-05-30 Minnesota Mining & Mfg Image forming composition
US4065315A (en) * 1976-04-26 1977-12-27 Dynachem Corporation Phototropic dye system and photosensitive compositions containing the same
US4280888A (en) * 1977-10-14 1981-07-28 W. R. Grace & Co. Screen printable, UV curable opaque legend ink composition
US4162162A (en) * 1978-05-08 1979-07-24 E. I. Du Pont De Nemours And Company Derivatives of aryl ketones and p-dialkyl-aminoarylaldehydes as visible sensitizers of photopolymerizable compositions
US4343885A (en) * 1978-05-09 1982-08-10 Dynachem Corporation Phototropic photosensitive compositions containing fluoran colorformer
US4341860A (en) * 1981-06-08 1982-07-27 E. I. Du Pont De Nemours And Company Photoimaging compositions containing substituted cyclohexadienone compounds
US4535052A (en) * 1983-05-02 1985-08-13 E. I. Du Pont De Nemours And Company Constrained n-alkylamino aryl ketones as sensitizers for photopolymer compositions
US4575625A (en) * 1983-09-27 1986-03-11 Knowles Carl H Integral hand-held laser scanner
JPS61160740A (en) * 1985-01-09 1986-07-21 Pilot Pen Co Ltd:The Photosensitive coloring composition
US4565769A (en) * 1984-11-21 1986-01-21 E. I. Du Pont De Nemours And Company Polymeric sensitizers for photopolymer composition
US4874799A (en) * 1985-05-17 1989-10-17 M&T Chemicals Inc. Aqueous akaline developable, UV curable urethane acrylate compounds and compositions useful for forming liquid 100 percent solids, solvent-free solder mask coatings
US4622286A (en) * 1985-09-16 1986-11-11 E. I. Du Pont De Nemours And Company Photoimaging composition containing admixture of leuco dye and 2,4,5-triphenylimidazolyl dimer
US4894314A (en) * 1986-11-12 1990-01-16 Morton Thiokol, Inc. Photoinitiator composition containing bis ketocoumarin dialkylamino benzoate, camphorquinone and/or a triphenylimidazolyl dimer
US4882265A (en) * 1988-05-18 1989-11-21 E. I. Du Pont De Nemours And Company Infrared laser recording film
US4987230A (en) * 1988-07-28 1991-01-22 E. I. Du Pont De Nemours And Company Photopolymerization sensitizers active at longer wavelengths
US4917977A (en) * 1988-12-23 1990-04-17 E. I. Du Pont De Nemours And Company Visible sensitizers for photopolymerizable compositions
US5102952A (en) * 1989-08-04 1992-04-07 Rohm And Haas Company Thermoplastic polymer compositions containing melt-rheology modifiers
US5219917A (en) * 1989-08-29 1993-06-15 Rohm And Haas Company Latex-paints
US5112721A (en) * 1990-01-29 1992-05-12 E. I. Du Pont De Nemours And Company Photopolymerizable compositions containing sensitizer mixtures
JPH03259138A (en) * 1990-03-08 1991-11-19 Fuji Photo Film Co Ltd Photoimage forming material
US5320933A (en) * 1990-03-30 1994-06-14 Morton International, Inc. Photoimageable composition having improved adhesion promoter
US5137571A (en) * 1990-06-05 1992-08-11 Rohm And Haas Company Method for improving thickeners for aqueous systems
US5149617A (en) * 1990-10-23 1992-09-22 Isp Investments Inc. Imageable diacetylene ethers
US5139928A (en) * 1990-10-23 1992-08-18 Isp Investments Inc. Imageable recording films
US5019549A (en) * 1990-10-25 1991-05-28 Kellogg Reid E Donor element for thermal imaging containing infra-red absorbing squarylium compound
US5516581A (en) * 1990-12-20 1996-05-14 Minnesota Mining And Manufacturing Company Removable adhesive tape
US5147758A (en) * 1991-02-19 1992-09-15 E. I. Du Pont De Nemours And Company Red sensitive photopolymerizable compositions
US5153106A (en) * 1991-03-11 1992-10-06 Isp Investments Inc. Direct color imaging with laser in a writing mode
JPH04369639A (en) * 1991-06-19 1992-12-22 Kimoto & Co Ltd Image forming material
US5256520A (en) * 1991-12-20 1993-10-26 E. I. Du Pont De Nemours And Company Visible photosensitizers for photopolymerizable compositions
US5204467A (en) * 1991-12-20 1993-04-20 E. I. Du Pont De Nemours And Company Visible photosensitizers for photopolymerizable compositions
JPH05210343A (en) * 1992-01-31 1993-08-20 Fujitsu Ltd Hologram forming material and production of hologram
JPH05210344A (en) * 1992-01-31 1993-08-20 Fujitsu Ltd Hologram forming material and production of hologram
US5236808A (en) * 1992-04-13 1993-08-17 E. I. Du Pont De Nemours And Company Visible photosensitizers for photopolymerizable compositions
US5484927A (en) * 1992-04-13 1996-01-16 E. I. Du Pont De Nemours And Company Visible dye photosensitizers derived from tropinone
JP2753918B2 (en) * 1992-05-26 1998-05-20 富士写真フイルム株式会社 Image forming material
US5395718A (en) * 1992-11-18 1995-03-07 The Boeing Company Conformal photolithographic method and mask for manufacturing parts with patterned curved surfaces
JP2751089B2 (en) * 1992-11-30 1998-05-18 大日本インキ化学工業株式会社 Laser marking method and printing ink
TW245844B (en) * 1993-01-29 1995-04-21 Komatsu Mfg Co Ltd
JPH07126559A (en) * 1993-11-04 1995-05-16 Showa Denko Kk Light-decolorable recording material
US6326450B1 (en) * 1994-02-22 2001-12-04 Moore Business Forms Activated adhesive system
US5414041A (en) * 1994-04-08 1995-05-09 Rohm And Haas Company Waterborne coating composition
JP2830756B2 (en) * 1994-11-10 1998-12-02 株式会社デンソー Laser marking method
US5764390A (en) * 1994-12-23 1998-06-09 Lucent Technologies Inc. Holographic method for generating three dimensional conformal photo-lithographic masks
US6632522B1 (en) * 1995-02-16 2003-10-14 3M Innovative Properties Company Blended pressure-sensitive adhesives
JPH08218037A (en) * 1995-02-16 1996-08-27 Rohm & Haas Co Water paint composition
US5665522A (en) * 1995-05-02 1997-09-09 Minnesota Mining And Manufacturing Company Visible image dyes for positive-acting no-process printing plates
WO1996039646A1 (en) * 1995-06-05 1996-12-12 Kimberly-Clark Worldwide, Inc. Novel pre-dyes
US5786132A (en) * 1995-06-05 1998-07-28 Kimberly-Clark Corporation Pre-dyes, mutable dye compositions, and methods of developing a color
JPH0934110A (en) * 1995-07-17 1997-02-07 Konica Corp Photopolymerizable composition, method for generating radical, photosensitive material for producing planographic printing plate, and production of planographic printing plate using the same
US5942554A (en) * 1996-02-20 1999-08-24 Spectra Group Limited, Inc. Method for forming highly colored polymeric bodies
US5742385A (en) * 1996-07-16 1998-04-21 The Boeing Company Method of airplane interiors assembly using automated rotating laser technology
US5744280A (en) * 1996-09-05 1998-04-28 E. I. Du Pont De Nemours And Company Storage-stable photoimageable deutero leuco dye/photooxidation compositions with improved leuco dye
US5723653A (en) * 1996-12-09 1998-03-03 Rheox, Inc. Liquid rheological additives providing rheological properties to non-aqueous systems
JP3839541B2 (en) * 1997-02-24 2006-11-01 富士写真フイルム株式会社 Colored image forming material
US6187432B1 (en) * 1997-03-11 2001-02-13 Avery Dennison Corporation Composite pressure sensitive adhesive
US5955224A (en) * 1997-07-03 1999-09-21 E. I. Du Pont De Nemours And Company Thermally imageable monochrome digital proofing product with improved near IR-absorbing dye(s)
US5858583A (en) * 1997-07-03 1999-01-12 E. I. Du Pont De Nemours And Company Thermally imageable monochrome digital proofing product with high contrast and fast photospeed
JPH11109555A (en) 1997-10-02 1999-04-23 Fuji Photo Film Co Ltd Light image forming material
AU749794B2 (en) * 1997-10-23 2002-07-04 H.B. Fuller Company Hot melt pressure sensitive adhesive which exhibits minimal staining
US6251571B1 (en) * 1998-03-10 2001-06-26 E. I. Du Pont De Nemours And Company Non-photosensitive, thermally imageable element having improved room light stability
US6411362B2 (en) * 1999-01-04 2002-06-25 International Business Machines Corporation Rotational mask scanning exposure method and apparatus
JP4130030B2 (en) * 1999-03-09 2008-08-06 富士フイルム株式会社 Photosensitive composition and 1,3-dihydro-1-oxo-2H-indene derivative compound
US6541109B1 (en) * 1999-10-08 2003-04-01 3M Innovative Properties Company Release coating formulation providing low adhesion release surfaces for pressure sensitive adhesives
US6503621B1 (en) * 2000-02-08 2003-01-07 3M Innovative Properties Company Pressure sensitive adhesives and articles including radial block and acrylic polymers
JP4132547B2 (en) * 2000-03-01 2008-08-13 富士フイルム株式会社 Image forming material and planographic printing plate precursor using the same
JP2001249430A (en) * 2000-03-07 2001-09-14 Fuji Photo Film Co Ltd Image recording medium
US6482879B2 (en) * 2000-04-17 2002-11-19 General Electric Company Composition for laser marking
US6547397B1 (en) * 2000-04-19 2003-04-15 Laser Projection Technologies, Inc. Apparatus and method for projecting a 3D image
US6309797B1 (en) * 2000-04-26 2001-10-30 Spectra Group Limited, Inc. Selectively colorable polymerizable compositions
US6754551B1 (en) * 2000-06-29 2004-06-22 Printar Ltd. Jet print apparatus and method for printed circuit board manufacturing
US6350792B1 (en) * 2000-07-13 2002-02-26 Suncolor Corporation Radiation-curable compositions and cured articles
US6433035B1 (en) * 2000-08-14 2002-08-13 Spectra Group Limited, Inc. Selectively colorable polymerizable compositions
US6528555B1 (en) * 2000-10-12 2003-03-04 3M Innovative Properties Company Adhesive for use in the oral environment having color-changing capabilities
US6613381B1 (en) * 2000-10-20 2003-09-02 3M Innovative Properties Company Thermoplastic additives for hot melt adhesives based on non-thermoplastic hydrocarbon elastomers
US6545084B2 (en) * 2001-02-23 2003-04-08 Rohm And Haas Company Coating composition
JP2002308922A (en) * 2001-04-12 2002-10-23 Fuji Photo Film Co Ltd Photopolymerizable composition and recording material obtained by using the same
US6627309B2 (en) * 2001-05-08 2003-09-30 3M Innovative Properties Company Adhesive detackification
US7172991B2 (en) * 2001-10-11 2007-02-06 Hewlett-Packard Development Company, L.P. Integrated CD/DVD recording and labeling
US20030149164A1 (en) * 2002-01-18 2003-08-07 Minnee Marcel Jan Paint composition for a strippable decorative paint film
US6835789B1 (en) * 2003-06-18 2004-12-28 Loctite (R&D) Limited Cyanoacrylate compositions
WO2005027039A2 (en) 2003-09-08 2005-03-24 Laser Projection Technologies, Inc. 3d projection with image recording
US6828525B1 (en) * 2004-01-28 2004-12-07 The Boeing Company Method of assembling an article using laser light projection and a photoreactive material

Also Published As

Publication number Publication date
EP1562073A1 (en) 2005-08-10
JP2011053718A (en) 2011-03-17
KR20060041749A (en) 2006-05-12
CN1727996B (en) 2011-01-26
TW200602802A (en) 2006-01-16
JP2005234561A (en) 2005-09-02
US20050175929A1 (en) 2005-08-11
CN1727996A (en) 2006-02-01
CN1776522B (en) 2012-08-01
US7270932B2 (en) 2007-09-18
KR101183265B1 (en) 2012-09-14
JP4945680B2 (en) 2012-06-06

Similar Documents

Publication Publication Date Title
CN100353207C (en) Imaging methods
US5262275A (en) Flexographic printing element having an IR ablatable layer and process for making a flexographic printing plate
JP4606188B2 (en) Improved imaging composition and method
US20120128890A1 (en) Method for curing substances by uv radiation, device for carrying out said method and ink cured by uv radiation
JP4945680B2 (en) Image forming composition and image forming method
CN1214292C (en) Forming method for photoresist design and its laminating products
CN100549816C (en) Image forming composition is applied to mark goods on the base material and forming method thereof
JP2010024295A (en) Photocurable composition, ink composition and inkjet recording method using the ink composition
JP3993692B2 (en) Resist pattern forming method
US7223519B2 (en) Imaging compositions and methods
JP3838234B2 (en) Energy sensitive acid generator, acid generating method, and energy sensitive curable composition
JP2011208107A (en) Photocurable inkjet ink and method for producing polymer
JP2005194475A (en) Energy beam sensitive acid-forming agent, method for generating acid and energy beam curable composition
JP2006008587A (en) Energy ray-sensitive acid-generating agent, method for generating acid, and energy ray-sensitive curable composition
CN1088208C (en) Normal position synchronous photopolymerization photo-generating color imaging material composition and its preparing method and use
JPH09263063A (en) Composition for forming energy beam-sensitive line image, image forming medium using the same and image forming method
JPH1157583A (en) Coating device and production of color filter

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20120801

Termination date: 20140206